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Metabolic-associated fatty liver disease and sarcopenia: A double whammy
Aditya Viswanath1, Sherouk Fouda2, Cornelius James Fernandez3
1School of Medicine, Leicester University, Leicester LE1 7RH, United Kingdom.
Abstract:
The prevalence of metabolic-associated fatty liver disease (MAFLD) has increased substantially in recent years because of the global obesity pandemic. MAFLD, now recognized as the number one cause of chronic liver disease in the world, not only increases liver-related morbidity and mortality among sufferers but also worsens the complications associated with other comorbid conditions such as cardiovascular disease, type 2 diabetes mellitus, obstructive sleep apnoea, lipid disorders and sarcopenia. Understanding the interplay between MAFLD and these comorbidities is important to design optimal therapeutic strategies. Sarcopenia can be either part of the disease process that results in MAFLD (e.g., obesity or adiposity) or a consequence of MAFLD, especially in the advanced stages such as fibrosis and cirrhosis. Sarcopenia can also worsen MAFLD by reducing exercise capacity and by the production of various muscle-related chemical factors. Therefore, it is crucial to thoroughly understand how we deal with these diseases, especially when they coexist. We explore the pathobiological interlinks between MAFLD and sarcopenia in this comprehensive clinical update review article and propose evidence-based therapeutic strategies to enhance patient care.
Insights
Metabolic-associated fatty liver disease (MAFLD) and sarcopenia often coexist, impacting patient health. Understanding their complex relationship is key to developing effective treatments for these interconnected conditions.
Area of Science:
- Hepatology and Metabolic Disorders
- Geriatric Medicine
- Clinical Nutrition
Background:
- Metabolic-associated fatty liver disease (MAFLD) prevalence is rising globally due to obesity.
- MAFLD is the leading cause of chronic liver disease, exacerbating comorbidities like cardiovascular disease and type 2 diabetes.
- Sarcopenia, or muscle loss, is increasingly recognized as a significant factor in MAFLD progression.
Purpose of the Study:
- To elucidate the intricate pathobiological links between MAFLD and sarcopenia.
- To provide a comprehensive clinical update on managing coexisting MAFLD and sarcopenia.
- To propose evidence-based therapeutic strategies for patients with both conditions.
Main Methods:
- Comprehensive review of current clinical literature on MAFLD and sarcopenia.
- Analysis of pathobiological mechanisms connecting liver fat accumulation and muscle wasting.
- Synthesis of evidence for therapeutic interventions.
Main Results:
- Sarcopenia can be both a cause and consequence of MAFLD, particularly in advanced stages.
- The interplay between MAFLD and sarcopenia negatively impacts exercise capacity and disease outcomes.
- Muscle-related factors contribute to the worsening of MAFLD.
Conclusions:
- A thorough understanding of the MAFLD-sarcopenia axis is critical for effective patient management.
- Integrated therapeutic strategies addressing both conditions are necessary.
- Further research into optimizing treatment for coexisting MAFLD and sarcopenia is warranted.
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